Does BRENTUXIMAB VEDOTIN Cause Adverse event? 55 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 55 reports of Adverse event have been filed in association with BRENTUXIMAB VEDOTIN (ADCETRIS). This represents 0.6% of all adverse event reports for BRENTUXIMAB VEDOTIN.
55
Reports of Adverse event with BRENTUXIMAB VEDOTIN
0.6%
of all BRENTUXIMAB VEDOTIN reports
14
Deaths
31
Hospitalizations
How Dangerous Is Adverse event From BRENTUXIMAB VEDOTIN?
Of the 55 reports, 14 (25.5%) resulted in death, 31 (56.4%) required hospitalization, and 1 (1.8%) were considered life-threatening.
Is Adverse event Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for BRENTUXIMAB VEDOTIN. However, 55 reports have been filed with the FAERS database.
What Other Side Effects Does BRENTUXIMAB VEDOTIN Cause?
Off label use (1,370)
Neuropathy peripheral (695)
Pyrexia (693)
Febrile neutropenia (684)
Death (602)
Neutropenia (561)
Hodgkin's disease (512)
Nausea (392)
Diarrhoea (385)
Anaemia (374)
What Other Drugs Cause Adverse event?
ABATACEPT (4,028)
APIXABAN (3,871)
ETANERCEPT (3,096)
LENALIDOMIDE (2,426)
INFLIXIMAB (2,269)
ADALIMUMAB (2,121)
METHOTREXATE (1,846)
LEFLUNOMIDE (1,476)
RIVAROXABAN (1,465)
ALENDRONATE (1,462)
Which BRENTUXIMAB VEDOTIN Alternatives Have Lower Adverse event Risk?
BRENTUXIMAB VEDOTIN vs BREO ELLIPTA
BRENTUXIMAB VEDOTIN vs BREXANOLONE
BRENTUXIMAB VEDOTIN vs BREXPIPRAZOLE
BRENTUXIMAB VEDOTIN vs BREXUCABTAGENE AUTOLEUCEL
BRENTUXIMAB VEDOTIN vs BRIGATINIB